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LIVE POLIO IRUS VACCINES

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292 Efficacy-Laboratory Evidence<br />

TABLE 6. READMINISTRATION OF CHAT V<strong>IRUS</strong> THREE TO FIVE MONTHS AFTER BIRTH<br />

FIRST ADMINISTRATION<br />

SECOND ADMINISTRATION<br />

OUTCOME INFANTS REINFECTED POSITIVE ANTIBODY<br />

RESPONSE<br />

Infected,<br />

POSITIVE<br />

Antibody<br />

Response<br />

(No.)<br />

6<br />

2/6 3/6<br />

Infected,<br />

NO Antibody<br />

Response<br />

5<br />

5/5<br />

5/5<br />

NOT Infected,<br />

NO Antibody<br />

Response<br />

2<br />

0/2 0/2<br />

* Response in one infant uncertain.<br />

an antibody response after the first administration<br />

of virus, were readily reinfected in all five<br />

cases (Table 6). Excretion of virus after the<br />

second feeding was detected as long as the stools<br />

were examined (up to two weeks), despite a previous<br />

average excretion after the first feeding of<br />

over four weeks. That is to say, instead of having<br />

been rendered resistant to reinfection these<br />

five infants appeared to be as susceptible to infection<br />

as previously unexposed infants. However,<br />

the infants were not immunologically<br />

tolerant, as shown (Table 6) by the antibody response<br />

that followed reinfection in at least four<br />

of these five infants.<br />

SUMMARY AND CONCLUSION<br />

We found that neonatal premature infants were<br />

highly susceptible to infection with poliovirus,<br />

but that detectable antibody production was<br />

stimulated in only about half the instances of<br />

infection. The presence of passively acquired<br />

antibodies in the circulation of the infants seemed<br />

to have no effect on either intestinal infection or<br />

active antibody response to living attenuated<br />

poliovirus. Intestinal infection with the same<br />

virus was readily reestablished in infants who<br />

had previously been infected but were without<br />

antibodies, in contrast to the resistance to reinfection<br />

of successfully vaccinated premature<br />

infants. However, immunologic tolerance to<br />

poliovirus was not demonstrated, for all the infants<br />

who were infected were shown to be capable<br />

of an immune response to the attenuated poliovirus.<br />

ACKNOWLEDGMENTS<br />

The assistance of Walter Lauterer, M.D., Jane<br />

Sitnek, R.N., and Toby Goldschneider, and the<br />

cooperation of Paul Gyorgi, M.D., in carrying out<br />

this study, is gratefully acknowledged.<br />

REFERENCES<br />

1. Koprowski, H., Norton, T. W., Hummeler, K.,<br />

Stokes, Jr., J., Hunt, A. D., Flack, A., and<br />

Jervis, G. A.: Immunization of infants with<br />

living attenuated poliomyelitis virus. J. Am.<br />

M. Assn. 162: 1281-1288 (Dec. 1) 1956.<br />

2. Martins da Silva, M., McKelvey, J. L., Prem,<br />

K. A., Johnson, E. A., and Cox, H. R.: Immunization<br />

with orally administered attenuated<br />

live-virus poliomyelitis vaccine. Am. M.<br />

Assoc. J. Dis. Child. 96: 624-625 (Nov.) 1958.<br />

3. Plotkin, S. A., Koprowski, H., and Stokes, Jr.,<br />

J.: Clinical trials in infants of orally administered<br />

attenuated poliomyelitis viruses. Pediatrics<br />

23: 1041-1062 (June) 1959.

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